Role Description The primary responsibility of the Anesthesiologist ERT is to provide specialized medical care in emergency situations, ensuring the safe administration of anesthesia and pain management for patients undergoing critical interventions. You will collaborate closely with other healthcare professionals to stabilize patients and contribute to their overall well-being. - Emergency Anesthesia Administration - Quickly assess and prioritize patients in emergency situations requiring anesthesia. - Administer appropriate anesthesia techniques tailored to the specific needs of each patient. - Monitor patients closely during procedures to ensure their safety and adjust anesthesia levels as needed. - Trauma Stabilization - Participate in trauma resuscitation efforts, working in tandem with emergency physicians, surgeons, and other healthcare providers. - Contribute to the rapid assessment and stabilization of critically injured patients. - Critical Care Collaboration - Work closely with intensivists, emergency physicians, and surgeons to provide comprehensive care to critically ill patients. - Participate in multidisciplinary rounds and discussions to optimize patient management strategies. - Pain Management - Address acute pain issues in emergency situations, tailoring pain management strategies to individual patient needs. - Utilize regional anesthesia techniques when appropriate to enhance pain control. - Communication and Team Collaboration - Effectively communicate with other healthcare professionals to coordinate patient care. - Collaborate with nursing staff, respiratory therapists, and other team members to ensure seamless patient management. - Emergency Protocols and Preparedness - Stay informed about the latest emergency response protocols and guidelines. - Documentation and Record Keeping - Maintain accurate and timely documentation of procedures, medications administered, and patient responses. - Contribute to medical records to facilitate continuity of care. Perform other duties as assigned. The duties and responsibilities listed in this document are representative of the nature and level of work assigned and not necessarily all inclusive. Qualifications - Medical degree (MD or DO) with completion of an accredited anesthesiology residency program. - Board certification in Anesthesiology. - Current medical license. - Familiarity with emergency response protocols established by Jordanian healthcare authorities. - Experience in emergency medicine or critical care is highly desirable. - Strong interpersonal and communication skills. - Ability to make quick and sound decisions under pressure.

POSITION SUMMARY This role is Flex/Remote which allows most work to be performed at home or on occasion at a Cigna office location. Ideal candidate will reside within an hour of the Tempe, AZ or Warrendale PA site. The hours for this position are 11:00 AM to 8:00 pm EST for PA and 10:00 AM to 7:00 PM or 11:00 AM to 8:00P PA AZ time depending on Day Light Savings time for account for a 11:00 AM to 8:00 PM equivalent EST shift. The Staff Pharmacist interprets physicians’ prescriptions, contacts doctors or other prescribers and/or patients to verify information on prescriptions and expedite processing of order. This position is responsible for regulatory guidelines. The Staff Pharmacist will track order status and outstanding issues as well as consult with patients regarding the use of medications and potential drug interactions. This individual may take calls from customers regarding lost orders or dispensing errors, maintain daily production, quality and service levels, vary work priorities and activities to accommodate business needs. The Staff Pharmacist may also train less experienced pharmacists. ESSENTIAL FUNCTIONS o Provide oversight and quality assurance to pharmacy technicians. o Interpret physicians’ or prescribers’ prescriptions. o Contact doctors and/or patients to verify information on prescriptions such as drug strength, prescription sig., and drug name in order to expedite processing of orders. o Verify and confirm validity of controlled substances. o Verify prescription information entered in the system by data entry or order entry. o Contact physicians for new and/or transfer authorization. o Work with physicians to convert prescriptions to generic or preferred drugs whenever possible. o Consult with patients regarding the use of medications and potential drug interactions. o Back up other pharmacists as needed, perform additional duties as assigned by management, or train less experienced pharmacists. QUALIFICATIONS o Current resident pharmacist license in good standing. o Advanced problem solving skills and the ability to work collaboratively with other departments to resolve issues. o Good oral and written communication skills. o Ability to read and interpret prescriptions. o Strong focus on customer service, quality and accuracy. o Ability to manage timelines and meet tight client deadlines. o Ability to adapt in a changing environment. o Ability to work a flexible schedule for peak volume times. If you will be working at home occasionally or permanently, the internet connection must be obtained through a cable broadband or fiber optic internet service provider with speeds of at least 10Mbps download/5Mbps upload. About Evernorth Health Services Evernorth Health Services, a division of The Cigna Group, creates pharmacy, care and benefit solutions to improve health and increase vitality. We relentlessly innovate to make the prediction, prevention and treatment of illness and disease more accessible to millions of people. Join us in driving growth and improving lives. Qualified applicants will be considered without regard to race, color, age, disability, sex, childbirth (including pregnancy) or related medical conditions including but not limited to lactation, sexual orientation, gender identity or expression, veteran or military status, religion, national origin, ancestry, marital or familial status, genetic information, status with regard to public assistance, citizenship status or any other characteristic protected by applicable equal employment opportunity laws. If you require reasonable accommodation in completing the online application process, please email: SeeYourself@cigna.com for support. Do not email SeeYourself@cigna.com for an update on your application or to provide your resume as you will not receive a response. The Cigna Group has a tobacco-free policy and reserves the right not to hire tobacco/nicotine users in states where that is legally permissible. Candidates in such states who use tobacco/nicotine will not be considered for employment unless they enter a qualifying smoking cessation program prior to the start of their employment. These states include: Alabama, Alaska, Arizona, Arkansas, Delaware, Florida, Georgia, Hawaii, Idaho, Iowa, Kansas, Maryland, Massachusetts, Michigan, Nebraska, Ohio, Pennsylvania, Texas, Utah, Vermont, and Washington State. Qualified applicants with criminal histories will be considered for employment in a manner consistent with all federal, state and local ordinances.

• Assist in design, author and/or review clinical study synopses, protocols, amendments, study reports and other study-related documents. • Act as a medical monitor for assigned study. • Discuss study design with investigators and key opinion leaders. • Provide clinical input for clinical protocol monitoring guidelines and analysis plans. • Drive clinical database design, data collection and cleaning and oversees clinical interpretation of study data. • Track emerging efficacy and safety profile of drugs in on-going clinical trials; inform Clinical Development team of changes in the efficacy/safety and/or risk benefit profiles as they occur. • Provide input and/or prepare clinical sections of regulatory documents (e.g., INDs, IND annual reports, Investigator’s Brochures, CRFs, Informed Consent forms, Statistical Analysis Plans, Data Management edit check specs, clinical supplies package diagrams and labeling). • Lead or assist in the development of publications – abstracts, manuscripts, slides, etc. • In collaboration with team members (e.g., Clinical Operations, Data Management), assist in identifying/evaluating/monitoring vendors, monitoring clinical trial conduct/status. • Assist in database finalization, reviews of study results, results interpretation and CSR’s. • Assist in planning and presentation conduct of investigator meetings and Advisory Boards. • Oversee and manage vendor activities/deliverables as appropriate. • Present study results, as appropriate, to medical/scientific community at meetings and in published format.

• Bring medical and scientific expertise to the design, execution, and interpretation of FIH, Phase 1, and Phase 2 clinical studies ensuring patient safety and scientific integrity • Author and oversee key clinical documents — including protocols, amendments, informed consent forms, investigator brochures, clinical study reports, and regulatory submissions (e.g., INDs, CTAs, DSURs). Respond to health authority and IRB inquiries for respective studies • Review, analyze, and interpret emerging clinical data (safety, efficacy, PK/PD) to identify trends and issues, ensuring timely resolution through cross-functional collaboration • Provide ongoing data review to ensure study conduct aligns with protocol, patient safety standards, and data integrity expectations. Collaborate with Pharmacovigilance to ensure awareness of key safety and efficacy findings, supporting SAE review, narrative development, and safety governance activities • Contribute to and present scientific and clinical data internally and externally (e.g., investigator meetings, scientific conferences, manuscripts, regulatory interactions) • Contribute to vendor oversight to ensure consistency, quality, and scientific rigor across all clinical deliverables. Interact with investigators as needed, assist in site selection, and support training of sites at study start-up